A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv976765



Internal ID15924035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:151793297..151828253hg38UCSC Ensembl
Innerchr3:151511085..151546041hg19UCSC Ensembl
Innerchr3:152993775..153028731hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3834957
hg1934957
hg1834957
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592049
Supporting Variants
Samples
Known GenesAADAC, MIR548H2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv976765
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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